Evidence map›Paper›PMID 33762699›Full record

ArticleScientific reports2021

Prevalence of pathogenic copy number variants among children conceived by donor oocyte.

Sandra Monfort, Carmen Orellana, Silvestre Oltra, Mónica Rosello, Alfonso Caro-Llopis, Francisco Martinez

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Triplication of theGenes · 2024
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Sandra MonfortGenetics Unit, Hospital Universitario Y Politecnico La Fe, 46026, Valencia, Spain.
Carmen OrellanaGenetics Unit, Hospital Universitario Y Politecnico La Fe, 46026, Valencia, Spain.
Silvestre OltraGenetics Unit, Hospital Universitario Y Politecnico La Fe, 46026, Valencia, Spain.
Mónica RoselloGenetics Unit, Hospital Universitario Y Politecnico La Fe, 46026, Valencia, Spain.
Alfonso Caro-LlopisGenomics Unit, Instituto de Investigacion Sanitaria La Fe, Valencia, Spain.
Francisco MartinezGenetics Unit, Hospital Universitario Y Politecnico La Fe, 46026, Valencia, Spain. francisco@gva.es.
Hospital Universitari i Politècnic La Fe · ESInstituto de Investigación Sanitaria La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of assisted reproductive technologies to address infertility has favored the birth of many children in the last years. The majority of children born with these treatments are healthy, but some concerns remain on the safety of these medical procedures. We have retrospectively analyzed both the fertilization method and the microarray results in all those children born between 2010 and 2019 with multiple congenital anomalies, developmental delay and/or autistic spectrum disorder (n = 486) referred for array study in our center. This analysis showed a significant excess of pathogenic copy number variants among those patients conceived after in vitro fertilization with donor oocyte with respect to those patients conceived by natural fertilization (p = 0.0001). On the other hand, no significant excess of pathogenic copy number variants was observed among patients born by autologous oocyte in vitro fertilization. Further studies are necessary to confirm these results and in order to identify the factors that may contribute to an increased risk of genomic rearrangements, as well as consider the screening for genomic alterations after oocyte donation in prenatal diagnosis.

Indexed as

DNA Copy Number VariationsGenetic Predisposition to DiseaseChildChromosomes, Human, Pair 2FemaleFertilization in VitroHumansKaryotypingMaleOocytesPolymorphism, Single NucleotidePrevalenceReproductive Techniques, AssistedRisk AssessmentRisk Factors

Identifiers

PMID33762699
PMCPMC7991411
OpenAlexW3136093498

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.